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Evaluating Clinical Outcomes for Determining the Optimal Delay to Skin Incision Under WALANT

Evaluating Clinical Outcomes for Determining the Optimal Delay to Skin Incision Under WALANT: a Prospective Series of 34 Patients From a Low Resource Tertiary Setting

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04491656
Acronym
WALANT
Enrollment
34
Registered
2020-07-29
Start date
2019-01-01
Completion date
2020-07-15
Last updated
2020-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hand Surgery, Orthopedic Surgery

Brief summary

Further studies are needed to establish the effects of WALANT in performing most common hand surgeries, in relation to its clinical outcomes and intraoperative blood loss. Therefore, this study aims to identify the best interval time to perform elective hand surgeries using WALANT technique, document clinical outcomes and identify potential complications

Detailed description

To propose the optimal time delay from the injection to skin incision for most WALANT surgeries of the hand or wrist by analyzing not only intraoperative blood loss, but also postoperative pain scores and complication rates To determine if there is a difference between performing the WALANT technique with a waiting interval of 7 minutes as compared to 30 minutes prior to incision in relation to blood loss, pain scores, and complications. Initiate the use of WALANT technique and its application in practice of Orthopaedic Residents in East Avenue Medical Center

Interventions

A technique commonly used in hand surgeries where the combination of lidocaine and epinephrine is used for local blood control, thus performing the procedure without a tourniquet

Sponsors

East Avenue Medical Center, Philippines
Lead SponsorOTHER_GOV

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

1. . Signed Consent Form 2. Elective Hand Surgeries 3. Minor Hand Surgeries 4. Adult Male/Female ages 18 and above 5. Multiply injured

Exclusion criteria

1. No Consent 2. Multiply injured patient 3. Traumatic Hand Injuries 4. Known allergic reaction to either Epinephrine or Lidocaine. 5. Known heart condition 6. Patients on anticoagulants 7. Patients diagnosed with bleeding disorders

Design outcomes

Primary

MeasureTime frameDescription
VRS Score24 weeksVerbal Rating Scale 1. 0 for no pain 2. 1 for mild pain 3. 2 for moderate pain 4. 3 for severe pain 5. 4 for very severe pain

Secondary

MeasureTime frameDescription
Blood Loss24 weeksBlood loss estimation using Gauze Visual Analogue Scale by Algadiem et.al.

Other

MeasureTime frameDescription
Complications24 weeksComplications which may occur during the course of treatment and subsequent follow up of the patients which includes: wound complications, infection, stiffness, pain

Countries

Philippines

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026